References
- Long J, Yan S, Lao K, et al. The diagnosis and molecular analysis of a novel 21.9kb deletion (Qinzhou type deletion) causing α+ thalassemia. Blood Cells Mol Dis. 2014;52(4):225–229
- Long J, Ye X, Lao K, et al. Detection of three common α-thalassemia in non-deletion types and six common thalassemia in deletion types by QF-PCR. Clin Biochem. 2013;46(18):1860–1864
- Wei XF, Shang X, He DQ, et al. Molecular characterization of a novel 27.6-kb deletion causing α+ thalassemia in a Chinese family. Ann Hematol. 2011;90(1):17–22
- Lin M, Wu JR, Huang Y, et al. Clinical and molecular characterization of a rare 2.4 kb deletion causing α+ thalassemia in a Chinese family. Blood Cells Mol Dis. 2012;49(2):83–84
- Zhao JB, Zhao L, Fei YJ, et al. A novel α-thalassemia-2 (−2.7-kb) observed in a Chinese patient with Hb H disease. Am J Hematol. 1991;38(3):248–249
- Harteveld CL, Higgs DR. α-Thalassaemia. Orphanet J Rare Dis. 2010;5:13. doi: 10.1186/1750-1172-5-13